BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Agilon Moldable

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDIFLASH AND ESTEFLASH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    B-CARE5 (B-CARE5 SENSOR MODULE, VENOUS SENSOR, HOLDER FOR MEASURING HEAD)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    20 FR GASTROSTOMY TUBE

    FDA Adverse Event
    Malfunction ·ABBOTT NUTRITION·Product code KNT·October 7, 2008

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 27, 2013

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code IKX·August 5, 2011

    CLIP - EXACT CODE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·October 26, 2022

    HARMONIC ACE 5MM SHEAR

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 1, 2022